## Abstract The multicomponent reaction between oxopropylbenzoate(acetate) (I), (VI), primary amines (II), (N‐isocyanimino)triphenylphosphorane (III), and aromatic carboxylic acids (IV) proceeds smoothly at room temperature under neutral conditions to afford the sterically congested oxadiazole deri
A one-pot efficient four-component reaction for the synthesis of 2-(arylamino)-2-(5-aryl-1,3,4-oxadiazol-2-yl)propyl benzoate (or acetate) derivatives
✍ Scribed by Ali Ramazani; Yavar Ahmadi; Asemeh Mashhadi Malekzadeh; Aram Rezaei
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 165 KB
- Volume
- 22
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20735
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Reactions of (N‐isocyanimino) triphenylphosphorane with 2‐oxopropylbenzoate (or acetate) in the presence of aromatic carboxylic acids and primary amines proceed smoothly at room temperature and in neutral conditions to afford sterically congested 1,3,4‐oxadiazole derivatives in high yields. The reaction proceeds smoothly and cleanly under mild conditions, and no side reactions were observed. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 22:692–698, 2011; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.20735
📜 SIMILAR VOLUMES
Reactions of biacetyl (¼ butane-2,3-dione) with (N-isocyanimino)triphenylphosphorane in the presence of aromatic carboxylic acids proceed smoothly at room temperature and under neutral conditions to afford 3-(5-aryl-1,3,4-oxadiazol-2-yl)-3-hydroxybutan-2-one derivatives in high yields. Introduction
## Abstract The 1‐{[(1__H__‐1,2,3‐Triazol‐4‐yl)methoxy]phenyl}‐1__H__‐pyrazolo[1,2‐__b__]phthalazine‐5,10‐dione derivatives **5** were synthesized by a simple and efficient method, __i.e.__, by the four‐component, one‐pot condensation reaction of phthalohydrazide **4**, a (propargyloxy)benzaldehyde